Last synced on 14 November 2025 at 11:06 pm

VivaChek Ino Blood Glucose Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K160179
510(k) Type
Traditional
Applicant
Vivachek Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2017
Days to Decision
450 days
Submission Type
Summary

VivaChek Ino Blood Glucose Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K160179
510(k) Type
Traditional
Applicant
Vivachek Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2017
Days to Decision
450 days
Submission Type
Summary